Pharmacology 3b - Drug Metabolism

Anil Chopra

  1. To understand the general principals of xenobiotic (foreign chemical) biotransformation.
  2. Be able to describe the routes and biochemistry of Phase I metabolism.
  3. Be able to describe the routes and biochemistry of Phase II metabolism.
  4. To understand the importance of drug metabolism in pharmacology.

-Xenobiotics (i.e. foreign molecules) are generally lipophilic.

-Metabolism tends to reduce or eliminate pharmacological/toxicological activity.

-Metabolism converts lipophilic chemicals to polar derivatives (readily excreted).

The main site for “first pass” metabolism is the liver. It can however occur in other organs.

Prodrugs are drugs which are inactive unless they are metabolised by the body e.g. L-DOPA  Dopamine.

Phase I Metabolism

At this stage oxidation, reduction and hydrolysis take place. Oxidation and reduction create new functional groups, and hydrolysis unmasks them. Generally this inactivates chemicals (however it can activate some prodrugs). The polarity of the drug is not often changed.

In the liver it is mainly mediated by cytochrome P450. Numerous isoforms of P450 are present and each with different and overlapping substrate specificities – about 12 count for hepatic drug metabolism.

E.g. cytochrome P450 metabolism

RH + NADPH + O2 + H+====Cytochrome P450====> ROH + NADP+ + H2O

E.g. alcohol metabolism

Phase II Metabolism

A number of different reactions can occur in phase II metabolism. All of these use enzymes and also require a high energy interemediate:

Glucuronidation: Glucuronyl transferase

Acetylation: Acetyl transferase

Amino acid conjugation: Acyl transferase

Methylation: Glutathione-S-transferase

Sulphation: Sulphotransferase

Glutathione conjugation: methyl transferase

This is CONJUGATION. Once a drug has been conjugated, it is almost always less active and polar (and therefore ready for excretion).

Effects of Metabolism

The biological half-life of the chemical is decreased.

The duration of exposure is reduced.

Accumulation of the compound in the body is avoided.

Potency/duration of the biological activity of the chemical can be altered.

The pharmacology/ toxicology of the drug can be governed by its metabolism.

First pass metabolism is extensive metabolism in the liver before the drug reaches the systemic circulation after being taken orally.

Repeated administration of some drugs increases the synthesis of cytochrome-P450 (enzyme induction). This increases the rate of metabolism of this drug and others.

Some drugs inhibit microsomal activity and so act to increase the action of a drug – enzyme inhibition

Drug to dug interactions and genetic polymorphisms, age and some diseases especially those affecting the liver can also affect metabolism

Sometime reactive products of metabolism are toxic to various organs such as the liver. Paracetamol normally undergoes glucuronidation and sulphation, however with a high dose the livers stores of glutathione become depleted and a toxic metabolite accumulates